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Adsorption and heterogeneous reactions of ClONO2 and N2O5 on/with NaCl aerosol

机译:Clono2和N 2 O5对/含NaCl气溶胶的吸附和异质反应

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摘要

The adsorption and heterogeneous reactions of ClONO2 and N2O5 on the NaCl (100) surface have been investigated by performing density functional theory (DFT) calculations. Possible adsorption structures, energies and electronic properties of ClONO2 and N2O5 were studied by considering multiple possible adsorption sites without symmetry restriction. The most stable adsorption configurations are a vertical adsorption mode for ClONO2 and a horizontal adsorption mode for N2O5, with the adsorption energies of 14.81 and 13.67 kcal mol(-1), respectively. Two possible reactions were proposed on the NaCl (100) surface. Adsorbed ClONO2 and N2O5 could react with HCl or hydrolyze on the NaCl surface to form HNO3 and other gaseous species (Cl-2, HOCl and ClNO2). More importantly, ClONO2 and N2O5 can actively participate in the heterogeneous reaction with NaCl to generate Cl-2 and ClNO2, which could be photolyzed to produce reactive chlorine atoms. The adsorbed H2O molecule plays an important role in the key elementary step and promotes the formation of the products. The present results rationalize previous experimental studies well and enrich our understanding of the source of halogen atoms in the marine boundary layer.
机译:通过进行密度泛函理论(DFT)计算,研究了Clono2和N 2 O 5对NaCl(100)表面的吸附和异质反应。通过考虑没有对称限制的多种可能的吸附点,研究了Clono2和N2O5的可能吸附结构,能量和电子性质。最稳定的吸附配置是用于CLONO2的垂直吸附模式和N2O5的水平吸附模式,其吸附能量为14.81和13.67kcal摩尔(-1)。在NaCl(100)表面上提出了两种可能的反应。吸附的ClonO 2和N 2 O 5可以与HCl反应或在NaCl表面上水解以形成HNO 3和其它气态物质(Cl-2,HoCl和ClNO 2)。更重要的是,Clono2和N2O5可以积极参与与NaCl的异质反应以产生Cl-2和ClNO 2,这可以光解以产生反应性氯原子。吸附的H 2 O分子在关键的基本步骤中起重要作用,并促进了产品的形成。本结果将先前的实验研究吻合得很好,并丰富了我们对海域边界层中卤素原子源的理解。

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  • 来源
    《RSC Advances 》 |2016年第52期| 共9页
  • 作者单位

    Shandong Univ Environm Res Inst Jinan 250100 Peoples R China;

    Shandong Univ Environm Res Inst Jinan 250100 Peoples R China;

    Shandong Univ Environm Res Inst Jinan 250100 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学 ;
  • 关键词

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